Dye-sensitized photoelectric conversion device

ABSTRACT

The present invention relates to an organic dye-sensitized photoelectric conversion device and a solar cell utilizing the same. In accordance with a demand to now for development of an organic dye-sensitized photoelectric conversion device with high conversion efficiency and high practicability using an inexpensive dye, there is provided in the present invention, a photoelectric conversion device with high conversion efficiency by producing a photoelectric conversion device by sensitizing fine semiconductor particles with a methine dye having specified skeleton.

TECHNICAL FIELD

The present invention relates to an organic dye-sensitized photoelectric conversion device and a solar cell and more specifically, to a photoelectric conversion device characterized by using fine oxide semiconductor particles sensitized with a dye having specified skeleton and a solar cell utilizing the same.

PRIOR ART

Solar cells utilizing the sun light have been noticed as energy source substituting fossil fuel such as petroleum and coal. At present, solar cells using crystalline or amorphous silicon or compound semiconductor solar cells using such as gallium and arsenic have been developed and studied actively on efficiency enhancement. However, due to high energy and cost required to produce them, they have a problem of difficulty in general purpose applications. In addition to this problem, photoelectric conversion devices using dye-sensitized fine semiconductor particles or solar cells utilizing them are also known and materials and production technology to produce them have been disclosed (see JP No.2664194; B. O'Regan and M. Graetzel, Nature, vol. 353, p. 737 (1991); M. K. Nazeeruddin, A. Kay, I. Rodicio, R. Humphry-Baker, E. Muller, P. Liska, N. Vlachopoulos, M. Graetzel, J. Am. Chem. Soc., vol. 115, p. 6382 (1993)). These photoelectric conversion devices are produced using a relatively inexpensive oxide semiconductor such as titanium oxide and have potential to provide photoelectric conversion devices more inexpensive compared with conventional solar cells using silicon, and the like, and are noticed due to providing colorful solar cells. However, to obtain a highly efficient photoelectric conversion device, a ruthenium-based complex is used as a dye for sensitization, which has left problems of high cost of the dye itself and in supplying thereof. Use of an organic dye for sensitization has been challenged already, however, practical application has not been succeeded at present due to problems of low conversion efficiency, stability and durability, and thus further improvement of conversion efficiency is required (see WO 2002011213). Likewise, production examples of photoelectric conversion devices using a methine dye are known and relatively many studies have been carried out on a coumarin dye (JP-A-2002-164089) or a merocyanine dye (JP-A-8-81222, JP-A-11-214731 and JP-A-2001-52766), however, further improvement of cost, stability and conversion efficiency is required.

Thus, in a photoelectric conversion device using an organic dye-sensitized semiconductor, it is required to develop a photoelectric conversion device with high conversion efficiency and practicability using an inexpensive organic dye.

DETAILED DISCLOSURE OF THE INVENTION

The present inventors have studied comprehensively a way to solve the above problems and found that by producing a photoelectric conversion device by sensitization of fine semiconductor particles with a specified dye and thus have completed the present invention.

That is, the present invention provides the following aspects:

(1) A photoelectric conversion device, characterized by using fine oxide semiconductor particles sensitized with a methine dye represented by Formula (1):

(in Formula (1), each of R₁ and R₂ represents a hydrogen atom, an aromatic residual group which may have substituent(s), an aliphatic hydrocarbon residual group which may have substituent(s) or an acyl group, provided that R₁ and R₂ may form a ring which may have substituent(s), by bonding with each other or with a benzene ring a₁; m₁ is an integer of 0 to 7; n₁ is an integer of 1 to 7; X₁ represents an aromatic residual group which may have substituent(s), a cyano group, a phosphate group, a sulfo group, a carboxyl group, a carboamido group, an alkoxycarbonyl group or an acyl group; each of A₁ and A₂ represents independently an aromatic residual group which may have substituent(s), a hydroxyl group, a phosphate group, a cyano group, a hydrogen atom, a halogen atom, an aliphatic hydrocarbon residual group which may have substituent(s), a carboxyl group, a carboamido group, an alkoxycarbonyl group or an acyl group, provided that when n₁ is not smaller than 2 and A₁ and A₂ are present in plural, each of A₁ and each of A₂ may be the same or different each other. A ring which may have substituent(s) may be formed using multiple substituents selected from A₁ or each of A₁ when A₁ is present in plural, and A₂ or each of A₂ when A₂ is present in plural, along with X₁; Y₁ represents a sulfur atom, a selenium atom, a tellurium atom and CR₃R₄ or NR₅, wherein R₃ and R₄ represent a hydrogen atom, a halogen atom, an amide group, a hydroxyl group, a cyano group, a nitro group, an alkoxyl group, an acyl group, a substituted or unsubstituted amino group, an aliphatic hydrocarbon residual group which may have substituent(s) or an aromatic residual group which may have substituent(s); R₅ represents a hydrogen atom, an aromatic residual group which may have substituent(s), an aliphatic hydrocarbon residual group which may have substituent(s) or an acyl group; when m₁ is not smaller than 2 and Y₁ is present in plural, each of Y₁ may be the same or different each other; a benzene ring a₁ may have one or plural substituents, including a halogen atom, an amide group, a hydroxyl group, a cyano group, a nitro group, an alkoxyl group, an acyl group, a substituted or unsubstituted amino group, an aliphatic hydrocarbon residual group which may have substituent(s) or an aromatic residual group which may have substituent(s); a benzene ring a₁ may also form a ring which may have substituent(s) by bonding of plural substituents themselves; and a ring b₁ may have one or plural substituents including a halogen atom, an alkoxyl group, an acyl group, an aliphatic hydrocarbon residual group which may have substituent(s) or an aromatic residual group which may have substituent(s); and a ring b₁ may form a ring which may have substituent(s) by bonding of plural substituents themselves)

(2) The photoelectric conversion device according to the aspect (1), characterized that a methine dye represented by Formula (1) is a compound with R₁ and R₂ being an aromatic residual group which may have substituent(s) in Formula (1).

(3) The photoelectric conversion device according to the aspect (2), characterized that a methine dye represented by Formula (1) is a compound represented by Formula (2) as shown below.

(in Formula (2), m₂, n₂, X₂, A₃, A₄, Y₂, a₂ and b₂ represent the same meaning as corresponding m₁, n₁, X₁, A₁, A₂, Y₁, a₁ and b₁ in Formula (1); a benzene ring c₁ may further have one or plural substituents, including a halogen atom, an amide group, a hydroxyl group, an alkoxyl group, a substituted or unsubstituted amino group, an aliphatic hydrocarbon residual group which may have substituent(s) or an aromatic residual group which may have substituent(s), provided that the benzene ring c₁ may form a ring which may have substituent(s) by bonding of plural substituents themselves; each of R₆ and R₇ represents a substituted or unsubstituted amino group or an aromatic residual group which may have substituent(s)).

(4) The photoelectric conversion device according to the aspect (3), characterized that a methine dye represented by Formula (2) is a compound represented by Formula (3) as shown below.

(in Formula (3), m₃, n₃, X₃, A₅, A₆, Y₃, a₃ and b₃ represent the same meaning as corresponding m₁, n₁, X₁, A₁, A₂, Y₁, a₁ and b₁ in Formula (1); a benzene ring c₂ may further have one or plural substituents, including a halogen atom, an amide group, a hydroxyl group, an alkoxyl group, a substituted or unsubstituted amino group, an aliphatic hydrocarbon residual group which may have substituent(s) or an aromatic residual group which may have substituent(s), provided that the benzene ring c₂ may form a ring which may have substituent(s) by bonding of plural substituents themselves; each of R₁₁ and R₁₂ represents a substituted or un substituted amino group or an aromatic residual group which may have substituent(s)).

(5) The photoelectric conversion device according to the aspect (4), characterized that a methine dye represented by Formula (3) is a compound with R₁₁ and R₁₂ in Formula (3) being a substituted or unsubstituted amino group.

(6) The photoelectric conversion device according to the aspect (4), characterized that a methine dye represented by Formula (3) is a compound with R₁₁ and R₁₂ in Formula (3) being an aromatic residual group which may have substituent(s).

(7) The photoelectric conversion device according to the aspect (6), characterized that a methine dye represented by Formula (3) is a compound with X₃ in Formula (3) being a carboxyl group.

(8) The photoelectric conversion device according to the aspect (7), characterized that a methine dye represented by Formula (3) is a compound with X₃ in Formula (3) being a carboxyl group and A₆ at the nearest to X₃ being a cyano group, a carboxyl group or an acyl group.

(9) The photoelectric conversion device according to the aspect (6), characterized that a methine dye represented by Formula (3) is a compound with X₃ and A₆ at the most adjacent to X₃ in Formula (3) forming a ring which may have substituent(s).

(10) The photoelectric conversion device according to the aspects (1) to (9), characterized that a methine dye represented by Formula (3) is a compound with m₃ in Formula (3) being 1 to 3.

(11) The photoelectric conversion device according to the aspect (10), characterized that a methine dye represented by Formula (3) is a compound with n₃ in Formula (3) being 1 to 4.

(12) The photoelectric conversion device according to the aspects (1) to (11), characterized that a methine dye represented by Formula (3) is a compound with Y₃ in Formula (3) being a sulfur atom.

(13) A photoelectric conversion device, characterized by using an oxide semiconductor sensitized with one kind or more of a methine dye represented by Formula (1) and with a metal complex and/or an organic dye having a structure other than Formula (1).

(14) The photoelectric conversion device according to any one of the aspects (1) to (13), wherein fine oxide semiconductor particles contain titanium dioxide as an essential component.

(15) The photoelectric conversion device according to any one of the aspects (1) to (14), wherein fine oxide semiconductor particles contain zinc or tin as an essential component as a metal component.

(16) The photoelectric conversion device according to the aspects (1) to (15), wherein onto fine oxide semiconductor particles a dye is carried in the presence of an inclusion compound.

(17) A production method for a photoelectric conversion device, characterized by making fine oxide semiconductor particles, formed in a thin membrane, to carry a dye represented by Formula (1).

(18) A solar cell characterized by using a photoelectric conversion device according to any one of the aspects (1) to (16).

(19) Fine oxide semiconductor particles sensitized with a methine dye according to the above Formulas (1) to (3).

(20) A methine dye, characterized in that in the above Formula (1), R₁ and R₂ represent benzene rings; Y, represents a sulfur atom; m₁ is an integer of 1 to 2; n₁ is an integer of 1; X₁ represents a carboxyl group; A₁ represents a hydrogen atom; and A₂ represents a cyano group.

(21) A methine dye characterized in that in the above Formula (1), R₁ and R₂ represent benzene rings; Y₁ represents a sulfur atom; m₁ is an integer of 1 to 2; n₁ is an integer of 1; and X₁ and A₂ form a rhodanine ring.

(22) A methine dye characterized in that in the above Formula (3), R₁₁ and R₁₂ represent a substituted or unsubstituted amino group or an aromatic residual group which may have substituent(s); m₃ is an integer of 0 to 3; n₃ is an integer of 1 to 2; X₃ represents a carboxyl group; A₅ represents a hydrogen atom; and A₆ represents a cyano group.

Embodiments To Carry Out The Invention

The present invention is explained in detail below. A photoelectric conversion device of the present invention uses an oxide semiconductor sensitized with a dye represented by Formula (1) as shown below:

Each of R₁ and R₂ in Formula (1) represents a hydrogen atom, an aromatic residual group which may have substituent(s), an aliphatic hydrocarbon residual group which may have substituent(s) and an acyl group.

An aromatic residual group means an aromatic ring group from which a hydrogen atom is removed and includes, for example, aromatic hydrocarbon rings such as benzene, naphthalene, anthracene, phenanthrene, pyrene, perylene and terrylene; heterocyclic aromatic rings such as indene, azulene, pyridine, pyrazine, pyrimidine, pyrazole, pyrazolidine, thiazolidine, oxazolidine, pyran, chromene, pyrrol, pyrrolidine, benzimidazol, imidazoline, imidazolidine, imidazole, pyrazole, triazole, triazine, diazole, indoline, thiophene, furan, oxazole, thiazine, thiazole, indole, benzothiazole, naphthothiazole, benzoxazole, naphthoxazole, indolenine, benzoindolenine, pyrazine, quinoline and quinazoline; and fused aromatic rings such as fluorene and carbazole, and they may have substituent(s) as described above. Usually, it is preferable that they are aromatic residual groups having a C₅₋₁₆ aromatic ring (an aromatic ring or a fused ring containing an aromatic ring).

An aliphatic hydrocarbon residual group includes a saturated or unsaturated, linear, branched and cyclic alkyl group and preferably such one as have carbon atoms of 1 to 36, more preferably carbon atoms of 1 to 20. A cyclic group includes, for example, a C₃₋₈ cycloalkyl group. Specific examples include a methyl group, an ethyl group, a n-propyl group, an isopropyl group, a n-butyl group, an isobutyl group, a tert-butyl group, an octyl group, an octadecyl group, a cyclohexyl group, a propenyl group, a pentynyl group, a butenyl group, a hexenyl group, a hexadienyl group, an isopropenyl group, an isohexenyl group, a cyclohexenyl group, a cyclopentadienyl group, an ethynyl group, a propynyl group, a pentynyl group, a hexynyl group, an isohexynyl group and a cyclohexynyl group. They may have substituent(s) as described above.

An acyl group includes, for example, a C₁₋₁₀ alkylcarbonyl group, a C₁₋₁₀ arylcarbonyl group, preferably C₁₋₄ alkylcarbonyl group including typically such as an acetyl group, a trifluoromethylcarbonyl group and a propionyl group. An arylcarbonyl group includes a benzcarbonyl group, a naphthocarbonyl group, and the like.

A substituent in an aromatic residual group which may have substituent(s) and an aliphatic hydrocarbon residual group which may have substituent(s) is not especially limited but includes a hydrogen atom, a sulfo group, a sulfamoyl group, a cyano group, an isocyano group, a thiocyanato group, an isothiocyanato group, a nitro group, a nitrosyl group, a halogen atom, a hydroxyl group, a phosphono group, a phosphate group, a substituted or unsubstituted amino group, a mercapto group which may have substituent(s), an amido group which may have substituent(s), an alkoxy group which may have substituent(s), an aryloxy group which may have substituent(s), a substituted carbonyl group such as a carboxyl group, a carbamoyl group, an acyl group, an aldehyde group or an alkoxycarbonyl group, an aromatic residual group which may have substituent(s), an aliphatic hydrocarbon residual group which may have substituent(s). A halogen atom includes a fluorine atom, a chlorine atom, a bromine atom and an iodine atom. A phosphate group includes a (C₁₋₄) alkyl phosphate group. A substituted or unsubstituted amino group includes, for example, an amino group; an alkyl-substituted amino group such as a mono- or a dimethylamino group, a mono- or a diethylamino group and a mono- or a dipropylamino group; an aromatic substituted amino group such as a mono- or a diphenylamino group and a mono- or a dinaphthylamino group; an amino group substituted with one alkyl group and one aromatic hydrocarbon residual group, such as a monoalkyl monophenyl amino group; a benzylamino group or an acetylamino group and a phenylacetylamino group. A mercapto group which may have substituent(s) includes such as a mercapto group, an alkylmercapto group and a phenylmercapto group. An amido group which may be substituted includes such as an amido group, an alkylamido group and an arylamido group. An alkoxyl group means a group formed by bonding the above aliphatic hydrocarbon residual group with an oxygen atom including, for example, a methoxy group, an ethoxy group, a butoxy group a tert-butoxy group and an aryloxy group includes such as a phenoxy group and a naphthoxy group. They may have substituent(s) as described above. The substituent is a similar one as described in the item of an aromatic residual group which may have substituent(s). An acyl group is a similar one as described above. An alkoxycarbonyl group includes a C₁₋₁₀ alkoxycarbonyl group. An aromatic residual group which may have substituent(s) and an aliphatic hydrocarbon residual group which may have substituent(s) are similar ones as described above.

R₁ and R₂ may together form a ring which may have substituent(s), by bonding with each other or with a benzene ring a₁. A ring formed by bonding of R₁ and R₂ each other includes a morpholine ring, a piperidine ring, a piperazine ring, a pyrrolidine ring, a carbazole ring and an indole ring. A ring formed by bonding of R₁ or R₂ with a benzene ring a₁ includes a julolidine ring. They may have substituent(s) as described above. The substituent is a similar one as described in the item of an aromatic residual group which may have substituent(s) and an aliphatic hydrocarbon residual group which may have substituent(s).

R₁ and R₂ in Formula (1) are preferably an aromatic residual group which may have substituent(s).

The substituent thereof may be similar one as described in the item of an aromatic residual group which may have substituent(s) and an aliphatic hydrocarbon residual group which may have substituent(s) and preferably a substituted or unsubstituted amino group and an aromatic residual group which may have substituent(s);

m₁ is an integer of 0 to 7, preferably an integer of 0 to 6 and more preferably an integer of 1 to 3. n₁ is an integer of 1 to 7, preferably an integer of 1 to 6 and more preferably an integer of 1 to 4. Such a combination of m₁ and n₁ is particularly preferable as m₁ is an integer of 1 to 3 and n₁ is an integer of 1 to 4.

X₁ in Formula (1) represents an aromatic residual group which may have substituent(s), a cyano group, a phosphate group, a sulfo group; or a group having a substituted carbonyl group such as a carboxyl group, a carboamide group, an alkoxycarbonyl group and an acyl group. An aromatic residual group may be similar to one described above and the substituent which may be adopted may be similar to one as described in the item of an aromatic residual group which may have substituent(s). An alkoxycarbonyl group and an acyl group each may be similar to one described above. X₁ is preferably an aromatic residual group which may have substituent(s) or a carboxyl group and an aromatic residual group is preferably a residual group of salicylic acid or catechol. As is described later, X₁ may form a ring with A₁ or A₂. A ring to be formed is preferably a heterocycle residual group which may have substituent(s), including specifically pyridine, quinoline, pyran, chromene, pyrimidine, pyrrol, thiazole, benzothiazole, oxazole, benzoxazole, selenazole, benzoselenazole, imidazole, benzimidazole, pyrazole, thiophene and furan, and each heterocycle residual group may have more rings or may be hydrogenated or may be substituted as described above and also preferably has structure forming a rhodanine ring, an oxazolidone ring, a thiooxazolidone ring, a hydantoin ring, a thiohydantoin ring, an indandione ring, a thianaphthene ring, a pyrazolone ring, a barbituric ring, a thiobarbituric ring or a pyridone ring by bonding of these substituents thereof.

Each of A₁ and A₂ in Formula (1) independently represents an aromatic residual group which may have substituent(s), a hydroxyl group, a phosphate group, a cyano group, a hydrogen atom, a halogen atom, an aliphatic hydrocarbon residual group which may have substituent(s) or a group having a carbonyl group such as carboxyl group, a carboamide group, an alkoxycarbonyl group and an acyl group. An aromatic residual group, a halogen atom, an aliphatic hydrocarbon residual group, an alkoxycarbonyl group and an acyl group may be similar to one described above. When n₁ is not smaller than 2 and A₁ and A₂ are present in plural, each of A₁ and A₂ may independently be the same or different. It is preferable that each of A₁ and A₂ independently represents a hydrogen atom, a cyano group, an aliphatic hydrocarbon residual group, a halogen atom or a carboxyl group. A preferable combination is when n₁ is 1, both A₁ and A₂ are cyano groups, or A₁ is a hydrogen atom and A₂ is a hydrogen atom, a cyano group or a carboxyl group, or when n₁ is not smaller than 2, all of A₁s and A₂s are cyano groups, or all A₁s are hydrogen atoms and A₂ nearest to X₁ is a cyano group or a carboxyl group and other A₂s are hydrogen atoms. It is also preferable that A₁ in Formula (1), particularly when n₁ is not smaller than 2, A₁ most apart from X₁ is an aromatic residual group which may have substituent(s). An aromatic residual group may be similar to one described above and preferably to be a residual group of benzene, naphthalene, anthrathene, thiophene, pyrrole, furan, and the like. These aromatic residual groups may have substituent(s) as described above. The substituent is not especially limited and may be similar to one as described in the item of an aromatic residual group which may have substituent(s) and preferably a substituted or unsubstituted amino group or an aromatic residual group which may have substituent(s).

Also, a ring which may have substituent(s) may be formed using multiple substituents selected from A₁ or each of A₁ when A₁ is present in plural, and A₂ or each of A₂ when A₂ is present in plural, along with X₁.

It is particularly preferable that A₁ or each of A₁ when A₁ is present in plural, and A₂ or each of A₂ when A₂ is present in plural, form a ring which may have substituent(s), and a ring to be formed includes an unsaturated hydrocarbon ring or a heterocycle. An unsaturated hydrocarbon ring includes such as a benzene ring, a naphthalane ring, an anthracene ring, a phenanthrene ring, a pyrene ring, an indene ring, an azulene ring, a fluorene ring, a cyclobutene ring, a cyclohexene ring, a cyclopentene ring, a cyclohexadiene ring and a cyclopentadiene ring. A heterocycle includes such as a pyridine ring, a pyrazine ring, a piperidine ring, an indoline ring, a furan ring, a pyran ring, an oxazole ring, a thiazole ring, an indole ring, a benzothiazole ring, a benzoxazole ring, a quinoline ring, a carbazole ring and a benzopyran ring. Preferable ones among these include a benzene ring, a cyclobutene ring, a cyclopentene ring, a cyclohexene ring, a pyran ring and a furan ring. They may be substituted as described above. The substituent is a similar one as described in the item of an aromatic residual group which may have substituent(s) and an aliphatic hydrocarbon residual group which may have substituent(s). When they have a carbonyl group, a thiocarbonyl group, and the like, they may form a cyclic ketone or a cyclic thioketone, and these rings may have substituent(s). The substituents are similar ones as described in the item of an aromatic residual group which may have substituent(s) and an aliphatic hydrocarbon residual group which may have substituent(s).

When the heterocycle of above X₁ or the heterocycle formed by X₁ and A₁ and A₂ has a nitrogen atom, the nitrogen atom may be quaternary form and in that case may have a counter ion. The counter ion is not especially limited, however, it includes specifically such as F⁻, Cl⁻, Br⁻, I⁻, ClO₄ ⁻, BF₄ ⁻, PF₆ ⁻, OH⁻, SO₄ ²⁻, CH₃SO₄ and a toluene sulfonate ion, preferably Br⁻, I⁻, ClO₄ ⁻, BF₄ ⁻, PF₆ ⁻, CH₃SO₄ ⁻ and a toluene sulfonate ion. The nitrogen atom may also be neutralized by an acid group such as an intramolecular or intermolecular carboxyl group instead of the counter ion.

The above-described acid group such as a hydroxyl group, a phosphate group, a sulfo group and a carboxyl group each may form a salt, including a salt with an alkaline metal or an alkaline earth metal such as lithium, sodium, potassium, magnesium and calcium; or an organic base, for example, a salt such as a quaternary ammonium salt such as tetramethylammonium, tetrabutylammonium, pyridinium, imidazolium, piperazinium and piperidinium.

Y₁ in Formula (1) is a sulfur atom, a selenium atom, a tellurium atom, a group of CR₃R₄ or NR₅, and preferably a sulfur atom, a selenium atom, and more preferably a sulfur atom. R₃ and R₄ include a hydrogen atom, a halogen atom, an amido group, a hydroxyl group, a cyano group, a nitro group, an alkoxyl group, an acyl group, a substituted or unsubstituted amino group, an aliphatic hydrocarbon residual group which may have substituent(s) and an aromatic residual group which may have substituent(s). A halogen atom, an amido group, an alkoxyl group, an acyl group, a substituted or unsubstituted amino group, an aliphatic hydrocarbon residual group which may have substituent(s) and an aromatic residual group which may have substituent(s) each may be similar to one described above. R₅ includes a hydrogen atom, an aromatic residual group which may have substituent(s), an aliphatic hydrocarbon residual group which may have substituent(s) or an acyl group. The aromatic residual group which may have substituent(s), the aliphatic hydrocarbon residual group which may have substituent(s) or the acyl group may be similar one as described above. When m₁ is not smaller than 2 and Y₁ is present in plural, each of Y₁ may be the same or different. A benzene ring a₁ in Formula (1) may have 1 or plural substituents. The substituents may include a halogen atom, an amido group, a hydroxyl group, a cyano group, a nitro group, an alkoxyl group, an acyl group, a substituted or unsubstituted amino group, an aliphatic hydrocarbon residual group which may have substituent(s) and an aromatic hydrocarbon residual group which may have substituent(s), and when the benzene ring a₁ has plural substituents, a ring which may have substituent(s) may be formed by bonding of the plural substituents themselves. The ring to be formed includes the above-described saturated or unsaturated cyclic alkyl group, unsaturated hydrocarbon ring and heterocycle, which may have substituent(s) as described above. The substituent may be a similar one as described in the item of an aromatic residual group which may have substituent(s) and an aliphatic hydrocarbon residual group which may have substituent(s). A halogen atom, an amido group, an alkoxyl group, an acyl group, a substituted or unsubstituted amino group, an aliphatic hydrocarbon residual group which may have substituent(s) and an aromatic residual group which may have substituent(s) may each be a similar one as described above.

A ring b₁ in Formula (1) may have 1 or plural substituents. The substituents include a halogen atom, an alkoxyl group, an acyl group, an aliphatic hydrocarbon residual group which may have substituent(s) and an aromatic residual group which may have substituent(s). A halogen atom, an alkoxyl group, an acyl group, an aliphatic hydrocarbon residual group which may have substituent(s) and an aromatic residual group which may have substituent(s) may each be a similar one as described above.

A compound represented by Formula (1) may be present as a structural isomer such as cis-form and trans-form but is not especially limited and any of these can preferably be used as a photosensitizing dye.

A methine dye represented by Formula (1) is preferably a compound represented by the following Formula (2):

A₃ and A₄, m₂, n₂, X₂, Y₂, a benzene ring a₂ and a ring b₂ in Formula (2), have the same meanings as corresponding A₁ and A₂, m₁, n₁, X₁, Y1, a benzene ring a₁ and a ring b₁ in Formula (1). Each of R₆ and R₇ represents a substituted or unsubstituted amino group and an aromatic residual group which may have substituent(s). Each of a substituted or unsubstituted amino group and an aromatic residual group which may have substituent (s) is a similar one as described above.

A benzene ring c₁ may have 1 or plural substituents and as the substituents may have a halogen atom, an amido group, a hydroxyl group, an alkoxyl group, a substituted or unsubstituted amino group, an aliphatic hydrocarbon residual group which may have substituent(s) or an aromatic residual group which may have substituent(s), and when the benzene ring c₁ has plural substituents, a ring which may have substituent(s) may be formed by bonding of the plural substituents themselves. The ring to be formed includes the above-described saturated or unsaturated cyclic alkyl group, unsaturated hydrocarbon ring and heterocycle, which may have substituent(s) as described above. The substituent may be a similar one as described in the item of an aromatic residual group which may have substituent(s) and an aliphatic hydrocarbon residual group which may have substituent(s). A halogen atom, an amido group, an alkoxyl group, a substituted or unsubstituted amino group, an aliphatic hydrocarbon residual group which may have substituent(s) and an aromatic residual group which may have substituent(s) may each be a similar one as described above.

A methine dye represented by Formula (2) is preferably a compound represented by the following Formula (3):

A₅ and A₆, m₃, n₃, X₃, Y₃, a benzene ring a₃, a ring b₃, a benzene ring C₂, R₁₁ and R₁₂ in Formula (3) have the same meanings as corresponding A₃ and A₄, m₂, n₂, X₂, Y₂, a benzene ring a₂, a ring b₂, a benzene ring c₁, R₆ and R₇ in Formula (2).

The present invention further relates to methine compounds defined next and by using fine oxide semiconductor particles sensitized with these methine dyes, superior effect can be obtained.

(a) A methine dye represented by the above Formula (1) wherein R₁ and R₂ are benzene rings; Y₁ is a sulfur atom; m₁ is an integer of 1 to 2; n₁ is an integer of 1; X₁ is a carboxyl group; A₁ is a hydrogen atom; and A₂ is a cyano group.

(b) A methine dye represented by the above Formula (1), wherein R₁ and R₂ are benzene rings; Y₁ is a sulfur atom; m₁ is an integer of 1 to 2; n₁ is an integer of 1; and X₁ and A₂ form a rhodanine ring.

(c) A methine dye represented by the above Formula (3), wherein R₁₁ and R₁₂ are substituted or unsubstituted amino groups or an aromatic residual group which may have substituent(s); m₃ is an integer of 0 to 3; n₃ is an integer of 1 to 2; X₃ is a carboxyl group; A₅ is a hydrogen atom; and A₆ is a cyano group.

In a methine dye represented by Formula (1), wherein m₁ is 0, that is the following dye (7), can be produced by the following reaction scheme. Aniline is subjected to coupling by such as Ullman reaction to obtain an aniline derivative (4), followed by metallization using a base such as butyllithium, adopting a method for reaction with an amide derivative such as dimethylformamide or for reaction with Vilsmeier reagent obtained by reaction of such as dimethylformamide with such as phosphoryl chloride, to obtain a compound (5), a precursor of a compound (7). When n₁ is not smaller than 2, it can also be obtained by a method for Claisen condensation of a formyl group, a method for using an amido derivative such as dimethylaminoacrolein and dimethylaminovinylacrolein, and a method for subjecting a formyl group samely to Wittig reaction or Grignard reaction to obtain a vinyl group, followed by further formyl reaction above to obtain a propenal group, a pentadienal group, etc. Further, a dye (7) can be obtained by fusing a compound (5) and a compound (6) with an active methylene group in a solvent, for example, alcohols such as methanol, ethanol, isopropanol and butanol, aprotic polar solvents such as dimethylformamide and N-methylpyrrolidone; toluene and acetic anhydride; in the presence of a basic catalyst such as caustic soda, sodium methylate, sodium acetate, diethylamine, triethylamine, piperidine, piperazine and diazabicycloundecene, if necessary; at about 20° C. to 180° C., preferably at about 50° C. to 150° C. A dye (7) can also be obtained, when X₁ is a carboxyl group or a phosphate group, by reaction of an active methylene compound having an alkoxycarbonyl group or a phosphate group, respectively with a compound (5), followed by hydrolysis.

Compounds when m₁ is 0 are exemplified below.

Specific examples of dyes represented by the following Formula (8) are shown in Table 1 and Table 2, wherein a phenyl group is abbreviated as “Ph”. A ring of X₄ and a ring (a ring B) formed by X₄ with A₈ is shown below.

TABLE 1 (8)

Com pound n₄ R₁₆ R₁₇ R₁₈ R₁₉ R₂₀ R₂₁ A₇ A₈ X₄ 1 1 H H H H H H H H COOH 2 1 H H H H H H H CN COOH 3 1 CH₃ CH₃ CH₃ CH₃ H H H COOH COOH 4 1 CH₃ CH₃ CH₃ CH₃ H H H COOH COOH 5 1 CH₃ CH₃ CH₃ CH₃ H H H CF₃ COOH 6 1 CH₃ CH₃ CH₃ CH₃ H H H COCF₃ COOH 7 1 CH₃ CH₃ CH₃ CH₃ H H H COCH₃ COOH 8 1 CH₃ CH₃ CH₃ CH₃ H H H CN COOH 9 1 CH₃ CH₃ CH₃ CH₃ H H H CN COOCH₃ 10 1 CH₃ CH₃ CH₃ CH₃ H H H CN COOLi 11 1 CH₃ CH₃ CH₃ CH₃ H H H CN COONa 12 1 CH₃ CH₃ CH₃ CH₃ H H H CN COOK 13 1 CH₃ CH₃ CH₃ CH₃ H H H CN PO(OH)₂ 14 1 C₂H₅ C₂H₅ C₂H₅ C₂H₅ H H H CN COOH 15 1 C₄H₉ C₄H₉ C₄H₉ C₄H₉ H H H CN COOH 16 1 C₈H₁₇ C₈H₁₇ C₈H₁₇ C₈H₁₇ H H H CN COOH 17 1 Ph Ph Ph Ph H H H CN COOH 18 1 Ph CH₃ Ph CH₃ H H H CN COOH 19 1 Ph H Ph H H H H CN COOH 20 1 CH₃ CH₃ CH₃ CH₃ OCH₃ H H CN COOH 21 1 CH₃ CH₃ CH₃ CH₃ OH H H CN COOH 22 1 CH₃ CH₃ CH₃ CH₃ H CH₃ H CN COOH 23 1 CH₃ CH₃ CH₃ CH₃ H H CH₃ CN COOH 24 2 CH₃ CH₃ CH₃ CH₃ H H H H COOH 25 3 CH₃ CH₃ CH₃ CH₃ H H H H COOH 26 4 CH₃ CH₃ CH₃ CH₃ H H H H COOH 27 5 CH₃ CH₃ CH₃ CH₃ H H H H COOH 28 6 CH₃ CH₃ CH₃ CH₃ H H H H COOH 29 7 CH₃ CH₃ CH₃ CH₃ H H H H COOH

TABLE 2 Compound n₄ R₁₆ R₁₇ R₁₈ R₁₉ R₂₀ R₂₁ A₇ A₈ X₄ 30 1 CH₃ CH₃ CH₃ CH₃ H H H H Ring B₁ 31 1 CH₃ CH₃ CH₃ CH₃ H H H H Ring B₂ 32 1 CH₃ CH₃ CH₃ CH₃ H H H H Ring B₃ 33 1 CH₃ CH₃ CH₃ CH₃ H H H H Ring B₄ 34 1 CH₃ CH₃ CH₃ CH₃ H H H H Ring B₅ 35 1 CH₃ CH₃ CH₃ CH₃ H H H H Ring B₆ 36 1 CH₃ CH₃ CH₃ CH₃ H H H H Ring B₇ 37 1 CH₃ CH₃ CH₃ CH₃ H H H H Ring B₈ 38 1 CH₃ CH₃ CH₃ CH₃ H H H H Ring B₉ 39 1 CH₃ CH₃ CH₃ CH₃ H H H H Ring B₁₀ 40 1 CH₃ CH₃ CH₃ CH₃ H H H H Ring B₁₁ 41 1 C₂H₅ C₂H₅ C₂H₅ C₂H₅ H H H H Ring B₁₂ 42 1 C₄H₉ C₄H₉ C₄H₉ C₄H₉ H H H H Ring B₁₃ 43 1 C₈H₁₇ C₈H₁₇ C₈H₁₇ C₈H₁₇ H H H A₈ and X₄ form a ring B₁₄ 44 1 Ph Ph Ph Ph H H H A₈ and X₄ form a ring B₁₅ 45 1 Ph CH₃ Ph CH₃ H H H A₈ and X₄ form a ring B₁₆ 46 1 Ph H Ph H H H H A₈ and X₄ form a ring B₁₇ 47 1 CH₃ CH₃ CH₃ CH₃ H H H A₈ and X₄ form a ring B₁₈ 48 1 CH₃ CH₃ CH₃ CH₃ H H H A₈ and X₄ form a ring B₁₉ 49 1 CH₃ CH₃ CH₃ CH₃ H H H A₈ and X₄ form a ring B₂₀ 50 1 CH₃ CH₃ CH₃ CH₃ H H H A₈ and X₄ form a ring B₂₁ 51 1 CH₃ CH₃ CH₃ CH₃ H H H A₈ and X₄ form a ring B₂₂ 52 1 CH₃ CH₃ CH₃ CH₃ H H H A₈ and X₄ form a ring B₂₃ 53 1 CH₃ CH₃ CH₃ CH₃ H H H A₈ and X₄ form a ring B₂₄ 54 1 CH₃ CH₃ CH₃ CH₃ H H H A₈ and X₄ form a ring B₂₅ 55 1 CH₃ CH₃ CH₃ CH₃ H H H A₈ and X₄ form a ring B₂₆ 56 1 CH₃ CH₃ CH₃ CH₃ H H H A₈ and X₄ form a ring B₂₇ 57 1 CH₃ CH₃ CH₃ CH₃ H H H A₈ and X₄ form a ring B₂₈ 58 1 CH₃ CH₃ CH₃ CH₃ H H H A₈ and X₄ form a ring B₂₉

Other examples of dyes represented by Formula (8) are shown below.

Specific examples of dyes represented by the following Formula (9) are shown in Table 3 and Table 4, wherein a phenyl group is abbreviated as “Ph”. A ring of X₅ and a ring (a ring B) formed by X₅ with A₁₀ is shown below.

TABLE 3 (9)

compound n₅ R₂₂ R₂₃ R₂₄ R₂₅ R₂₆ R₂₇ A₉ A₁₀ X₅ 107 1 H H H H H H H H COOH 108 1 H H H H H H H CN COOH 109 1 H CH₃ H CH₃ H H H CN COOH 110 1 H H H H H H H COOH COOH 111 1 H H H H H H H CF₃ COOH 112 1 H H H H H H H COCF₃ COOH 113 1 H H H H H H H COCH₃ COOH 114 1 H Ph H Ph H H H CN COOH 115 1 H H H H H H H CN COOCH₃ 116 1 H H H H H H H CN COOLi 117 1 H H H H H H H CN COONa 118 1 H H H H H H H CN COOK 119 1 H H H H H H H CN PO(OH)₂ 120 1 CH₃ H CH₃ H H H H CN COOH 121 1 C₄H₉ H C₄H₉ H H H H CN COOH 122 1 C₈H₁₇ H C₈H₁₇ H H H H CN COOH 123 1 Cl H Cl H H H H CN COOH 124 1 Br H Br H H H H CN COOH 125 1 I H I H H H H CN COOH 126 1 H H H H OCH₃ H H CN COOH 127 7 H H H H OH H H CN COOH 128 1 H H H H H CH₃ H CN COOH 129 1 H H H H H H CH₃ CN COOH 130 2 H H H H H H H H COOH 131 3 H H H H H H H H COOH 132 4 H H H H H H H H COOH 133 5 H H H H H H H H COOH 134 6 H H H H H H H H COOH 135 7 H H H H H H H H COOH

TABLE 4 Compound n₅ R₂₂ R₂₃ R₂₄ R₂₅ R₂₆ R₂₇ A₉ A₁₀ X₅ 136 1 H H H H H H H H Ring B₁ 137 1 H H H H H H H H Ring B₂ 138 1 H H H H H H H H Ring B₃ 139 1 H H H H H H H H Ring B₄ 140 1 H H H H H H H H Ring B₅ 141 1 H H H H H H H H Ring B₆ 142 1 H H H H H H H H Ring B₇ 143 1 H H H H H H H H Ring B₈ 144 1 H H H H H H H H Ring B₉ 145 1 H H H H H H H H Ring B₁₀ 146 1 H H H H H H H H Ring B₁₁ 147 1 H H H H H H H H Ring B₁₂ 148 1 H H H H H H H H Ring B₁₃ 149 1 H H H H H H H A₁₀ and X₅ form a ring B₁₄ 150 1 H H H H H H H A₁₀ and X₅ form a ring B₁₅ 151 1 H H H H H H H A₁₀ and X₅ form a ring B₁₆ 152 1 H H H H H H H A₁₀ and X₅ form a ring B₁₇ 153 1 H H H H H H H A₁₀ and X₅ form a ring B₁₈ 154 1 H H H H H H H A₁₀ and X₅ form a ring B₁₉ 155 1 H H H H H H H A₁₀ and X₅ form a ring B₂₀ 156 1 H H H H H H H A₁₀ and X₅ form a ring B₂₁ 157 1 H H H H H H H A₁₀ and X₅ form a ring B₂₂ 158 1 H H H H H H H A₁₀ and X₅ form a ring B₂₃ 159 1 H H H H H H H A₁₀ and X₅ form a ring B₂₄ 160 1 H H H H H H H A₁₀ and X₅ form a ring B₂₅ 161 1 H H H H H H H A₁₀ and X₅ form a ring B₂₆ 162 1 H H H H H H H A₁₀ and X₅ form a ring B₂₇ 163 1 H H H H H H H A₁₀ and X₅ form a ring B₂₈ 164 1 H H H H H H H A₁₀ and X₅ form a ring B₂₉

Other examples of dyes represented by Formula (9) are shown below.

A dye (1) in a methine dye represented by Formula (1), wherein m₁ is not smaller than 1, can be produced by the following reaction scheme. A compound (14), an intermediate for synthesis of a methine dye represented by Formula (1) can be produced generally by a method of Ogura, et al. (for example, see JP-A-2000-252071) (a compound (10) is converted to a boric acid derivatized compound (11), followed by reaction thereof with a compound (12)) (in the following reaction scheme, Z in a compound (12) represents a halogen atom such as Cl, Br and I.). Further by metallization of a compound represented by this Formula (13) using a base such as butyllithium, followed by reaction with an amide derivative such as dimethylformamide, or by reaction with Vilsmeier reagent, obtained by reaction of such as dimethylformamide with such as phosphoryl chloride, a compound (14), a precursor of a compound (1) can be obtained. When n₁ is not smaller than 2, it can also be obtained by a method for Claisen condensation of a formyl group and the like, amethod for using an amido derivative such as dimethylaminoacrolein and dimethylaminovinylacrolein, and amethod for subjecting a formyl group to Wittig reaction or Grignard reaction to obtain a vinyl group, followed by further formyl reaction above to obtain a propenal group, a pentadienal group, etc. Further, by fusing a compound (14) and a compound (6) having an active methylene group in a solvent, for example, alcohols such as methanol, ethanol, isopropanol and butanol, aprotic polar solvents such as dimethylformamide and N-methylpyrrolidone, toluene, acetic anhydride, and the like; in the presence of a basic catalyst such as caustic soda, sodium methylate, sodium acetate, diethylamine, triethylamine, piperidine, piperazine and diazabicycloundecene, if necessary; at 20° C. to 180° C., preferably at about 50° C. to 150° C., a dye (1) can be obtained. When X₁ is a carboxyl group or a phosphate group, by reaction of an active methylene compound having an alkoxycarbonyl group or a phosphate group, respectively with a compound (14), followed by hydrolysis, a compound (1) can also be obtained.

Compounds are exemplified below.

Specific examples of dyes represented by the following Formula (15) are shown in Table 5 to Table 7, wherein a phenyl group is abbreviated as “Ph”. A ring of X₆ and a ring (a ring B) formed by X₆ with A₁₂ is shown below.

TABLE 5 (15)

Com- pound m₄ n₆ R₂₆ R₂₉ R₃₀ R₃₁ Y₄ A₁₁ A₁₂ X₆ 193 1 1 H H H H S H H COOH 194 1 1 H H H H Se H OH COOH 195 1 1 H H H H NH H H COOH 196 1 1 H H H H NCH₃ H H COOH 197 1 1 CH₃ CH₃ H H S H CN COOH 198 1 1 CH₃ CH₃ H H Se H CONH₂ COOH 199 1 1 C₂H₅ C₂H₅ H H S H CN COOH 200 1 1 C₂H₅ C₂H₅ H H Te H CN COOH 201 1 1 C₃H₇ C₃H₇ H NO₂ S H CN COOH 202 1 1 C₄H₉ C₄H₉ H H S H CN COOH 203 1 1 C₈H₁₇ C₈H₁₇ H H S H CN COOH 204 1 1 C₁₈H₃₇ C₁₈H₃₇ H H S H CN COOH 205 1 1 Ph Ph H H S H CN COOH 206 1 1 Ph H H H S H CN COOH 207 1 1 Ph CH₃ H H S H CN COOH 208 1 1 Ph C₂H₅ H H S H CN COOH 209 1 1 Ph C₁₈H₃₇ H H S H CN COOH 210 1 1 CH₃ C₂H₅ H Cl S H CN COOH 211 1 1 COCH₃ C₂H₅ H H S H CN COOH 212 1 1 CH₃ CH₃ H H S CH₃ CN COOH 213 1 1 CH₃ CH₃ H CN S C₄H₉ CN COOH 214 1 1 CH₃ CH₃ H H S C₈H₁₇ CN COOH 215 1 1 CH₃ CH₃ H OCH₃ S H CN COOH 216 1 1 CH₃ CH₃ H OC₂H₅ S H CN COOH 217 1 1 Ph Ph H OC₈H₁₇ S H CN COOH 218 1 1 Ph Ph H OH S H CN COOH 219 1 1 Ph Ph CH₃ CH₃ S H CN COOH 220 1 1 Ph Ph NHCOCH₃ OCH₃ S H CN COOH 221 1 1 Ph Ph CH₃ Ph S H CN COOH 222 1 1 Ph Ph H H S H COOH COOH 223 1 1 Ph Ph H H S H CN COOLi 224 1 1 Ph Ph H COCH₃ S H CN COONa 225 1 1 Ph Ph H H S H CN COOK

TABLE 6 Compound m₄ n₆ R₂₈ R₂₉ R₃₀ R₃₁ Y₄ A₁₁ A₁₂ X₆ 226 1 1 Ph Ph H C₈H₁₇ S H CN COOH 227 1 1 Ph Ph H H S H CN PO(OH)₂ 228 1 1 Ph Ph H H S H CF₃ COOH 229 1 1 Ph Ph H H S H COCH₃ COOH 230 1 1 Ph Ph H H S H COCF₃ COOH 231 1 1 Ph Ph Ph Ph S H CN SO₃H 232 1 1 Ph Ph H H S H NO₂ COOH 233 1 1 Ph Ph H H S H CN COOCH₃ 234 1 1 Ph Ph H H S H COOCH₃ COOCH₃ 235 1 1 Ph Ph H H S H Cl COOH 236 1 1 Ph Ph H H S CH₃ CH₃ COOH 237 1 1 Ph Ph H H S Ph H CONH₂ 238 1 2 Ph Ph H N(CH₃)₂ S H H COOH 239 1 2 Ph Ph H H S CH₃ H COOH 240 1 2 Ph Ph H H S H CH₃ COOH 241 1 3 Ph Ph H H S H H COOH 242 1 4 Ph Ph H H S H H COOH 243 1 5 Ph Ph H H S H H COOH 244 1 7 Ph Ph H H S H H COOH 245 2 1 CH₃ CH₃ H H S H CN COOH 246 2 1 Ph Ph H H S H CN COOH 247 2 1 Ph Ph H H S CH₃ CN COOH 248 3 1 Ph Ph H H S H CN COOH 249 4 1 Ph Ph H H S H CN COOH 250 5 1 Ph Ph H H S H CN COOH 251 7 1 Ph Ph H H S H CN COOH 252 2 2 Ph Ph H H S H H COOH 253 3 2 Ph Ph H H S H H COOH 254 4 2 Ph Ph H H S H H COOH 255 5 2 Ph Ph H H S H H COOH

TABLE 7 Compound m₄ n₆ R₂₈ R₂₉ R₃₀ R₃₁ Y₄ A₁₁ A₁₂ X₆ 256 1 1 Ph Ph H H S H H Ring B₁ 257 1 1 Ph Ph H H S H H Ring B₂ 258 1 1 Ph Ph H H S H H Ring B₃ 259 1 1 Ph Ph H H S H H Ring B₄ 260 1 1 Ph Ph H H S H H Ring B₅ 261 1 1 Ph Ph H H S H H Ring B₆ 262 1 1 Ph Ph H H S H H Ring B₇ 263 1 1 Ph Ph H H S H H Ring B₈ 264 1 1 Ph Ph H H S H H Ring B₉ 265 1 1 Ph Ph H H S H H Ring B₁₀ 266 1 1 Ph Ph H H S H H Ring B₁₁ 267 1 1 Ph Ph H H S H H Ring B₁₂ 268 1 1 Ph Ph H H S H H Ring B₁₃ 269 1 1 Ph Ph H H S H A₁₂ and X₆ form a ring B₁₄ 270 1 1 Ph Ph H H S H A₁₂ and X₆ form a ring B₁₅ 271 1 1 Ph Ph H H S H A₁₂ and X₆ form a ring B₁₆ 272 1 1 Ph Ph H H S H A₁₂ and X₆ form a ring B₁₇ 273 1 1 Ph Ph H H S H A₁₂ and X₆ form a ring B₁₈ 274 1 1 Ph Ph H H S H A₁₂ and X₆ form a ring B₁₉ 275 1 1 Ph Ph H H S H A₁₂ and X₆ form a ring B₂₀ 276 1 1 Ph Ph H H S H A₁₂ and X₆ form a ring B₂₁ 277 1 1 Ph Ph H H S H A₁₂ and X₆ form a ring B₂₂ 278 1 1 Ph Ph H H S H A₁₂ and X₆ form a ring B₂₃ 279 1 1 Ph Ph H H S H A₁₂ and X₆ form a ring B₂₄ 280 1 1 Ph Ph H H S H A₁₂ and X₆ form a ring B₂₅ 281 1 1 Ph Ph H H S H A₁₂ and X₆ form a ring B₂₆ 282 1 1 Ph Ph H H S H A₁₂ and X₆ form a ring B₂₇ 283 1 1 Ph Ph H H S H A₁₂ and X₆ form a ring B₂₈ 284 1 1 Ph Ph H H S H A₁₂ and X₆ form a ring B₂₉

Specific examples of dyes represented by the following Formula (16) are shown in Table 8 and Table 9, wherein a phenyl group is abbreviated as “Ph”. A ring of X₇ and a ring (a ring B) formed by X₇ with A₁₄ is shown below.

TABLE 8 (16)

Com- pound m₅ n₇ R₃₂ R₃₃ R₃₄ R₃₅ R₃₆ R₃₇ Y₅ A₁₃ A₁₄ X₇ 285 1 1 H H H H H H S H H COOH 286 1 1 H H H H H H NH H H COOH 287 1 1 H H H H H H NCH₃ H H COOH 288 1 1 H H H H H H NPh H H COOH 289 1 1 H H H H H H S H CN COOH 290 1 1 H H CH₃ CH₃ CH₃ CH₃ S H CN COOH 291 1 1 H H CH₃ CH₃ CH₃ CH₃ NH H CN COOH 292 1 1 H H CH₃ CH₃ CH₃ CH₃ NCH₃ H CN COOH 293 1 1 H H CH₃ CH₃ CH₃ CH₃ NPh H CN COOH 294 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H CN COOH 295 1 1 H H C₃H₇ C₃H₇ C₃H₇ C₃H₇ S H CF₃ COOH 296 1 1 H H C₄H₉ C₄H₉ C₄H₉ C₄H₉ S H CN COOH 297 1 1 H H C₈H₁₇ C₈H₁₇ C₈H₁₇ C₈H₁₇ S H CN COOH 298 1 1 H H C₁₈H₃₇ C₁₈H₃₇ C₁₈H₃₇ C₁₈H₃₇ S H CN COOH 299 1 1 H H Ph Ph Ph Ph S H CN COOH 300 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S CH₃ CN COOH 301 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S F CN COOH 302 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S Cl CN COOH 303 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S Br CN COOH 304 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S I CN COOH 305 1 1 H OH C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H CN COOH 306 1 1 CH₃ H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H CN COOH 307 1 1 CH₃ OCH₃ C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H CN COOH 308 1 1 CH₃ C₈H₁₇ C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H CN COOH 309 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H COOH COOH 310 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H COONa COONa 311 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H CN COOLi 312 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H CN COONa 313 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H CN COOK 314 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H CN PO(OH)₂ 315 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H COCH₃ COOH 316 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H COCF₃ COOH 317 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H COCH₂F COOH 318 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H COCHF₂ COOH 319 2 1 H H Ph Ph Ph Ph S H H COOH 320 3 1 H H Ph Ph Ph Ph S H H COOH

TABLE 9 Compound m₅ n₇ R₃₂ R₃₃ R₃₄ R₃₅ R₃₆ R₃₇ Y₅ A₁₃ A₁₄ X₇ 321 4 1 H H Ph Ph Ph Ph S H H COOH 322 5 1 H H Ph Ph Ph Ph S H H COOH 323 6 1 H H Ph Ph Ph Ph S H H COOH 324 1 2 H H Ph Ph Ph Ph S H H COOH 325 1 3 H H Ph Ph Ph Ph S H H COOH 326 1 4 H H Ph Ph Ph Ph S H H COOH 327 1 5 H H Ph Ph Ph Ph S H H COOH 328 1 6 H H Ph Ph Ph Ph S H H COOH 329 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H CN Ring B₁ 330 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H CN Ring B₂ 331 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H CN Ring B₃ 332 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H CN Ring B₄ 333 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H CN Ring B₅ 334 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H CN Ring B₆ 335 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H CN Ring B₇ 336 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H CN Ring B₈ 337 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H CN Ring B₉ 338 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H CN Ring B₁₀ 339 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H CN Ring B₁₁ 340 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H CN Ring B₁₂ 341 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H CN Ring B₁₃ 342 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H A₁₄ and X₇ form a ring B₁₄ 343 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H A₁₄ and X₇ form a ring B₁₅ 344 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H A₁₄ and X₇ form a ring B₁₆ 345 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H A₁₄ and X₇ form a ring B₁₇ 346 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H A₁₄ and X₇ form a ring B₁₈ 347 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H A₁₄ and X₇ form a ring B₁₉ 348 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H A₁₄ and X₇ form a ring B₂₀ 349 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H A₁₄ and X₇ form a ring B₂₁ 350 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H A₁₄ and X₇ form a ring B₂₂ 351 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H A₁₄ and X₇ form a ring B₂₃ 352 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H A₁₄ and X₇ form a ring B₂₄ 353 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H A₁₄ and X₇ form a ring B₂₅ 354 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H A₁₄ and X₇ form a ring B₂₆ 355 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H A₁₄ and X₇ form a ring B₂₇ 356 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H A₁₄ and X₇ form a ring B₂₈ 357 1 1 H H C₂H₅ C₂H₅ C₂H₅ C₂H₅ S H A₁₄ and X₇ form a ring B₂₉ Specific examples of dyes represented by the following Formula (17) are shown in Table 10 and Table 11, wherein a phenyl group is abbreviated as “Ph”. X₃ and a ring (a ring B) formed by X₃ with A₈ is shown below.

TABLE 10 (17)

Com- pound m₆ n₈ R₃₈ R₃₉ R₄₀ R₄₁ R₄₂ R₄₃ Y₆ A₁₅ A₁₆ X₈ 358 1 1 H H H H H H S H H COOH 359 1 1 H H H H H H NH H H COOH 360 1 1 H H H H H H NCH₃ H H COOH 361 1 1 H H H H H H NPh H H COOH 362 1 1 H H H H H H S H CN COOH 363 1 1 H H H H H H S H CN COOH 364 1 1 H H CH₃ CH₃ CH₃ CH₃ NH H CN COOH 365 1 1 H H CH₃ CH₃ CH₃ CH₃ NCH₃ H CN COOH 366 1 1 H H H CH₃ H CH₃ S H CN COOH 367 1 1 H H H C₂H₅ H₅ C₂H₅ S H CN COOH 368 1 1 H H H C₃H₇ H C₃H₇ S H CN COOH 369 1 1 H H H C₄H₉ H C₄H₉ S H CN COOH 370 1 1 H H H C₈H₁₇ H C₈H₁₇ S H CN COOH 371 1 1 H H H C₁₈H₃₇ H C₁₈H₃₇ S H CN COOH 372 1 1 H H H Ph H Ph S H CN COOH 373 1 1 H H H C₂H₅ H C₂H₅ S CH₃ CN COOH 374 1 1 H H H C₂H₅ H C₂H₅ S F CN COOH 375 1 1 H H H C₂H₅ H C₂H₅ S Cl CN COOH 376 1 1 H H H C₂H₅ H C₂H₅ S Br CN COOH 377 1 1 H H H C₂H₅ H C₂H₅ S I CN COOH 378 1 1 H OH H C₂H₅ H C₂H₅ S H CN COOH 379 1 1 CH₃ H H C₂H₅ H C₂H₅ S H CN COOH 380 1 1 CH₃ OCH₃ H C₂H₅ H C₂H₅ S H CN COOH 381 1 1 CH₃ C₈H₁₇ H C₂H₅ H C₂H₅ S H CN COOH 382 1 1 H H H C₂H₅ H C₂H₅ S H COOH COOH 383 1 1 H H H C₂H₅ H C₂H₅ S H COONa COONa 384 1 1 H H H C₂H₅ H C₂H₅ S H CN COOLi 385 1 1 H H H C₂H₅ H C₂H₅ S H CN COONa 386 1 1 H H H C₂H₅ H C₂H₅ S H CN COOK 387 1 1 H H H C₂H₅ H C₂H₅ S H CN PO(OH)₂ 388 1 1 H H H C₂H₅ H C₂H₅ S H COCH₃ COOH 389 1 1 H H H C₂H₅ H C₂H₅ S H COCF₃ COOH 390 1 1 H H H C₂H₅ H C₂H₅ S H COCH₂F COOH 391 1 1 H H H C₂H₅ H C₂H₅ S H COCHF₂ COOH 392 2 1 H H H Ph H Ph S H H COOH 393 3 1 H H H Ph H Ph S H H COOH 394 4 1 H H H Ph H Ph S H H COOH

TABLE 11 Compound M₆ n₈ R₃₈ R₃₉ R₄₀ R₄₁ R₄₂ R₄₃ Y₆ A₁₅ A₁₆ X₈ 395 5 1 H H H Ph H Ph S H H COOH 396 6 1 H H H Ph H Ph S H H COOH 397 1 2 H H H Ph H Ph S H H COOH 398 1 3 H H H Ph H Ph S H H COOH 399 1 4 H H H Ph H Ph S H H COOH 400 1 5 H H H Ph H Ph S H H COOH 401 1 6 H H H Ph H Ph S H H COOH 402 1 1 H H H H H H S H CN Ring B₁ 403 1 1 H H H H H H S H CN Ring B₂ 404 1 1 H H H H H H S H CN Ring B₃ 405 1 1 H H H H H H S H CN Ring B₄ 406 1 1 H H H H H H S H CN Ring B₅ 407 1 1 H H H H H H S H CN Ring B₆ 408 1 1 H H H H H H S H CN Ring B₇ 409 1 1 H H H H H H S H CN Ring B₈ 410 1 1 H H H H H H S H CN Ring B₉ 411 1 1 H H H H H H S H CN Ring B₁₀ 412 1 1 H H H H H H S H CN Ring B₁₁ 413 1 1 H H H H H H S H CN Ring B₁₂ 414 1 1 H H H H H H S H CN Ring B₁₃ 415 1 1 H H H H H H S H A₁₆ and X₄ form a ring B₁₄ 416 1 1 H H H H H H S H A₁₆ and X₄ form a ring B₁₅ 417 1 1 H H H H H H S H A₁₆ and X₄ form a ring B₁₆ 418 1 1 H H H H H H S H A₁₆ and X₄ form a ring B₁₇ 419 1 1 H H H H H H S H A₁₆ and X₄ form a ring B₁₈ 420 1 1 H H H H H H S H A₁₆ and X₄ form a ring B₁₉ 421 1 1 H H H H H H S H A₁₆ and X₄ form a ring B₂₀ 422 1 1 H H H H H H S H A₁₆ and X₄ form a ring B₂₁ 423 1 1 H H H H H H S H A₁₆ and X₄ form a ring B₂₂ 424 1 1 H H H H H H S H A₁₆ and X₄ form a ring B₂₃ 425 1 1 H H H H H H S H A₁₆ and X₄ form a ring B₂₄ 426 1 1 H H H H H H S H A₁₆ and X₄ form a ring B₂₅ 427 1 1 H H H H H H S H A₁₆ and X₄ form a ring B₂₆ 428 1 1 H H H H H H S H A₁₆ and X₄ form a ring B₂₇ 429 1 1 H H H H H H S H A₁₆ and X₄ form a ring B₂₈ 430 1 1 H H H H H H S H A₁₆ and X₄ form a ring B₂₉

Other examples of dyes represented by Formulas (15) to (17) are shown below.

Structures of rings B are shown below.

A dye-sensitized photoelectric conversion device of the present invention is made by subjecting fine oxide semiconductor particles to carry a dye represented by Formula (1). In a preferred embodiment, a dye-sensitized photoelectric conversion device of the present invention is made by producing a thin film of an oxide semiconductor on a substrate using fine oxide semiconductor particles, followed by subjecting this film to carrying a dye represented by Formula (1).

A substrate for making thin film of an oxide semiconductor thereon, in the present invention, preferably has electric conductivity at the surface, and such a substrate is easily available on the market. Specifically, for example, such one as has a thin film of an electric conductive metal oxide such as tin oxide doped with indium, fluorine or antimony, or of a metal such as copper, silver and gold, which are formed on the surface of glass or transparent polymeric materials such as polyethylene terephthalate and polyether sulfone can be used. Electric conductivity thereof is usually not higher than 1000Ω and particularly preferably not higher than 100Ω.

As fine oxide semiconductor particles, a metal oxide is preferable, including specifically an oxide of such as titanium, tin, zinc, tungsten, zirconium, gallium, indium, yttrium, niobium, tantalum and vanadium. Among these, oxides of titanium, tin, zinc, niobium, indium, and the like are preferable and titanium oxide, zinc oxide and tin oxide are most preferable among them. These oxide semiconductors can be used alone or also by mixing thereof or coating of the semiconductor surface. Average particle diameter of fine oxide semiconductor particles is usually 1 to 500 nm, preferably 1 to 100 nm. These fine oxide semiconductor particles can also be used by mixing or making a multilayer of those with large particle diameter and those with small particle diameter.

A thin film of an oxide semiconductor can be produced by a method for forming a thin film on a substrate by spraying of fine oxide semiconductor particles; a method for electrical deposition of a thin film of fine semiconductor particles on a substrate as an electrode; and a method for hydrolysis of slurry of fine semiconductor particles or precursors of fine semiconductor particles such as semiconductor alkoxide to obtain paste containing fine particles, followed by coating on a substrate, drying, hardening or firing. A method for using slurry is preferable in view of performance of an oxide semiconductor electrode. In this method, slurry is obtained by dispersing secondary agglomerated fine oxide semiconductor particles in a dispersing medium by a common method so as to obtain average primary particle diameter of 1 to 200 nm.

Any dispersing medium to disperse slurry may be used as long as it can disperse fine semiconductor particles, and water, alcohols such as ethanol, ketones such as acetone and acetylacetone, and hydrocarbons such as hexane are used. They may be used as a mixture and use of water is preferable in view of suppressing viscosity change of slurry. Also to stabilize dispersion state of fine oxide semiconductor particles, a dispersion stabilizer can be used. A typical example of the dispersion stabilizer includes, for example, an acid such as acetic acid, hydrochloric acid and nitric acid; and acetylacetone, acrylic acid, polyethylene glycol, polyvinyl alcohol, etc.

A substrate coated with slurry may be fired and firing temperature is usually not lower than 100° C., preferably not lower than 200° C., and upper limit thereof is not higher than about melting point (softening point) of a substrate, usually 900° C., preferably not higher than 600° C. That is, firing time in the present invention is not especially limited, and, it is preferably within about 4 hours. Thickness of a thin film on a substrate is usually 1 to 200 μm, preferably 1 to 50μm. When firing is carried out, a thin film of fine oxide semiconductor particles is partially melt welded but such melt welding is not any obstacle to the present invention.

A thin film of an oxide semiconductor may be subjected to secondary treatment, that is, by directly dipping the thin film along with a substrate in a solution of an alkoxide, a chloride, a nitrate, a sulfate, and the like of the same metal as a semiconductor, followed by drying or re-firing, performance of a semiconductor thin film can be enhanced. The metal alkoxide includes such as titanium ethoxide, titanium isopropoxide, titanium tert-butoxide and n-dibutyl-diacetyl tin, and an alcohol solution thereof is used. The chloride includes, such as titanium tetrachloride, tin tetrachloride and zinc dichloride, and an aqueous solution thereof is used. Thus obtained oxide semiconductor thin film is consisted of fine oxide semiconductor particles.

Then, a method for subjecting fine oxide semiconductor particles formed in thin film state to carrying a dye is explained. A method for carrying a methine dye represented by Formula (1) includes a method for dipping a substrate formed with the above oxide semiconductor thin film in a solution obtained by dissolving said dye in a good solvent or, a dispersing liquid obtained by dispersing the dye when the dye has low solubility. Concentration in a solution or dispersion liquid is determined by a dye, as appropriate. Into such a solution, a semiconductor thin film formed on a substrate is dipped. Dipping time is from about room temperature to boiling point of the solvent, and dipping time is from 1 minute to about 48 hours. A typical example of a solvent used to dissolve a dye includes methanol, ethanol, acetonitrile, dimethylsulfoxide, dimethylformamide, acetone, t-butanol, etc. Concentration of a dye in a solution is usually 1×10⁻⁶ M to 1 M, preferably 1×10⁻⁵ M to 1×10⁻¹ M. In such conditions, a photoelectric conversion device of the present invention, containing thin film state fine oxide semiconductor particles sensitized with a dye can be obtained.

A methine dye represented by Formula (1) to be carried may be one kind or a mixture of several kinds. The mixture may be prepared using various dyes of the present invention themselves or with other dyes or metal complex dyes. In particular, by mixing dyes with different absorption wavelength, wide absorption wavelength can be utilized and thus a solar cell with high conversion efficiency can be obtained. Examples of metal complex dyes to be mixed are not especially limited, and, include preferably a ruthenium complex shown in M. K. Nazeeruddin, A. Kay, I. Rodicio, R. Humphry-Baker, E. Muller, P. Liska, N. Vlachopoulos, M. Graetzel, J. Am. Chem. Soc., vol.115, 6382 (1993) or a quaternary salt thereof, phthalocyanine and porphyrin. An organic dye used as a mixture includes phthalocyanine which contains no metal, porphyrin and cyanine, merocyanine, oxonol, triphenylmethane type, a methine type such as acrylic acid dye disclosed in WO 2002011213, a xanthene type, an azo type, an anthraquinone type, and a perylene type. Preferably, a ruthenium complex, merocyanine or a methine dye such as acrylic acid dye, and the like are included. When two or more kinds of dyes are used, these dyes may be adsorbed sequentially on a semiconductor thin film or adsorbed after mixing and dissolving them.

Mixing ratio of these dyes is not limited and optimally selected depending on each of the dyes and is preferably from equal molar ratio to preferably not less than about 10% by mole by one dye generally. When a dye is subjected to adsorption on fine oxide semiconductor particles using a solution mixed of or dispersed with various dyes, total concentration of the dyes in the solution may be similar to one in carrying only one kind. As a solvent when dyes are used in mixture, such a solvent as described above can be used and the solvents for each dye to be used may be the same or different.

When a dye is carried on a thin film of fine oxide semiconductor particles, to prevent aggregation of dyes themselves, it is effective to carry the dyes in the presence of an inclusion compound. In this case, the inclusion compound includes a steroid type compound such as cholic acid, crown ether, cyclodextrin, calixarene and polyethylene oxide, and preferably includes cholic acid derivatives such as deoxycholic acid, dehydrodeoxycholic acid, chenodeoxycholic acid, cholic acid methyl ester and cholic acid sodium salts; polyethylene oxide, etc. After the carrying of a dye, the surface of a semiconductor electrode may be treated with an amine compound such as 4-tert-butylpyridine or a compound having an acidic group such as acetic acid, propionic acid, etc. A method for treatment includes, for example, a method for dipping a substrate, formed with a thin film of fine semiconductor particles carrying a dye, in an ethanol solution of an amine.

A solar cell of the present invention is composed of an electrode (cathode) of a photoelectric conversion device, that is the above fine oxide semiconductor particles carrying a dye, a counter electrode (anode), a redox electrolyte or a positive hole transportation material or a p-type semiconductor, and the like. Morphology of a redox electrolyte or a positive hole transportation material or a p-type semiconductor, and the like includes liquid, solidified substance (gel or gel-like substance), solid, and the like. The liquid-like morphology includes a solution of a redox electrolyte, a molten salt, a positive hole transportation material, a p-type semiconductor, and the like in a solvent, a molten salt at normal temperature, and the like. The solidified substance morphology (gel or gel-like substance) includes those containing these in polymer matrix or a low molecular weight gelling agent, and the like. As the solid morphology, a redox electrolyte, a molten salt, a positive hole transportation material, a p-type semiconductor, and the like can be used. The positive hole transporting material includes amine derivatives; electric conductive polymers such as polyacetylene, polyaniline and polythiophene; and discotic liquid crystals such as a triphenylene type compound. The p-type semiconductor includes CuI, CuSCN, and the like. As the counter electrode, such one is preferable as has electric conductivity and acts catalytically for reduction reaction of the redox electrolyte and such one can be used as glass or a polymer film on which platinum, carbon, rhodium, ruthenium, and the like are vapor depositioned or fine conductive particles are coated.

The redox electrolyte used as a solar cell of the present invention includes a halogen-type redox electrolyte comprising a halogen compound having a halogen ion as a counter ion and a halogen molecule; a metal redox-type electrolyte of a metal complex such as a ferrocyanide-ferricyanide salt or a ferrocene-ferricinium ion and a cobalt complex; an organic redox-type electrolyte such as an alkyl thiol-alkyl disulfide, a viologen dye, hydroquinone-quinone, and a halogen-type redox electrolyte is preferable. In the halogen-type redox electrolyte comprising a halogen compound and a halogen molecule, a halogen molecule includes such as an iodine molecule and a bromine molecule, and an iodine molecule is preferable. The halogen compound having a halogen ion as a counter ion includes, for example, a salt of a metal halide such as LiI, NaI, KI, CsI, CaI₂, MgI₂ and CuI or an organic quaternary ammonium salt such as tetraalkylammonium iodide, imidazolium iodide and pyridinium iodide, and a salt having an iodide ion as a counter ion is preferable. Salts having an iodide ion as a counter ion include, for example, lithium iodide, sodium iodide and trimethylammonium iodide.

When the redox electrolyte takes a solution form containing it, an electrochemically inert solvent is used including, for example, acetonitrile, propylene carbonate, ethylene carbonate, 3-methoxypropionitrile, methoxyacetonitrile, ethylene glycol, propylene glycol, diethylene glycol, triethylene glycol, γ-butyrolactone, dimethoxyethane, diethyl carbonate, diethyl ether, dimethyl carbonate, 1,2-dimethoxyethane, dimethylformamide, dimethylsulfoxide, 1,3-dioxolan, methyl formate, 2-methyltetrahydrofuran, 3-methoxy-oxazolidine-2-one, sulpholane, tetrahydrofuran and water, and among them, such as acetonitrile, propylene carbonate, ethylene carbonate, 3-methoxypropionitrile, methoxyacetonitrile, ethylene glycol, 3-methoxy-oxazolidine-2-one and γ-butyrolactone are particularly preferable. These solvents may be used alone or in combination of two or more kinds. The gel-like redox electrolyte includes matrix such as an oligomer, a polymer, and the like containing the electrolyte or an electrolyte solution; a low molecular weight gelling agent described in W. Kubo, K. Murakoshi, T. Kitamura, K. Hanabusa, H. Shirai and S. Yanagida, Chem. Lett., p.1241 (1998), and the like, similarly containing the electrolyte or an electrolyte solution; and the like. Concentration of the redox electrolyte is usually 0.01 to 99% by weight, preferably 0.1 to 90% by weight.

A solar cell of the present invention is composed of a photoelectric conversion device (cathode) carrying a dye on fine oxide semiconductor particles on a substrate and a counter electrode (anode) placed opposing to the cathode, and can be prepared by filling a solution containing the redox electrolyte between them.

EXAMPLES

The present invention is explained in more detail in reference to the following Examples, however, the scope of the present invention should not be limited thereto. In Examples, “parts” means “mass parts” unless otherwise specified. Absorption spectra, nuclear magnetic resonance spectra and luminescence spectra were measured using a UV-visible ray spectrometer (JASCO V-570 from JASCO), a nuclear magnetic resonance measurement instrument (Gemini 300 from Varian Inc.) and a spectrofluorometer (JASCO FP-6600 from JASCO), respectively.

Example 1

One part of the following compound (532) and 0.45 parts of methyl cyanoacetate were dissolved in 10 parts of ethanol, followed by the addition of 0.05 parts of anhydrous piperazine thereto. After reaction under reflux for 2 hours, the reaction liquid was cooled to obtain a solid, which was filtered, washed and dried. This solid was reacted in 20 parts of ethanol in the presence of 1 part of potassium hydroxide under reflux for 2 hours. To the reaction solution was added 50 parts of water, followed by neutralization with hydrochloric acid and filtering orange crystal deposited, which was washed with water and further re-crystallized in ethanol to obtain 0.71 g of a compound (197) as orange brown crystal.

λmax (EtOH: 435 nm)

¹H-NMR (PPM: d6-DMSO): 2.97(s.CH₃.6H), 6.77(d.arom.2H), 7.42(d.thio.1H), 7.56(d.arom.2H), 7.66(d.thio.1H), 8.08(s.—CH═.1H)

Example 2

By similar treatment as in Synthesis Example 1 except that one part of the compound (532) was changed to 1.6 parts of the following compound (533), 0.98 g of a compound (205) was obtained as orange brown crystal.

λmax (EtOH: 431 nm)

¹H-NMR(PPM:d6-DMSO): 6.98(d.arom.2H), 7.12(m.arom.6H), 7.37(m.arom.4H), 7.64(d.thio.1H), 7.69(d.arom.2H), 8.00(d.thio.1H),8.47(s.—CH═.1H)

Example 3

By similar treatment as in Synthesis Example 1 except that one part of the compound (532) was changed to 1.7 parts of the following compound (534), 1.23 g of a compound (523) was obtained as brown crystal.

λmax (EtOH: 457 nm)

¹H-NMR (PPM: d6-DMSO): 6.98(d.arom.2H), 7.01-7.20(m.(arom.6H+—CH═.1H)), 7.27-7.44(m.(arom.4H+—CH═.1H)), 7.64(d.thio.1H), 7.68(d.arom.2H), 7.99(d.thio.1H), 8.47(s.—CH═.1H)

Example 4

By similar treatment as in Synthesis Example 1 except that one part of the compound (532) was changed to 1.9 parts of the following compound (535), 1.40 g of a compound (246) was obtained as brown crystal.

λmax (EtOH: 460 nm), the maximum luminescence (EtOH: 621 nm)

¹H-NMR (PPM: d6-DMSO): 6.97(d.arom.2H), 7.08(m.arom.6H), 7.35(m.arom.4H), 7.49(d.thio.1H), 7.58(d.thio.1H), 7.62(d.thio.1H), 7.62(d.arom.2H), 7.94(d.thio.1H), 8.43(s.—CH═.1H)

Example 5

One part of the compound (533) and 0.83 parts of rhodanine-3-acetic acid were dissolved in 10 parts of ethanol, followed by reaction under reflux for 2 hours. The reaction liquid was cooled to obtain a solid, which was filtered, washed, dried and further re-crystallized in ethanol to obtain 1.54 g of a compound (272) as brown crystal.

λmax (EtOH: 476 nm)

¹H-NMR (PPM: d6-DMSO): 4.71(s.CH₂.2H), 6.97(d.arom.2H), 7.12(m.arom.6H), 7.36(m.arom.4H), 7.66(d.thio.1H), 7.72(d.arom.2H), 7.82(d.thio.1H),8.16(s.—CH═.1H)

Example 6

By similar treatment as in Synthesis Example 1 except that one part of the compound (532) was changed to 1.7 parts of the following compound (536), 1.23 g of a compound (14) was obtained as brown crystal.

λmax (EtOH: 422 nm)

Example 7

By similar treatment as in Synthesis Example 1 except that one part of the compound (532) was changed to 1.9 parts of the following compound (537), 1.23 g of a compound (91) was obtained as brown crystal.

λmax (EtOH: 451 nm)

Example 8

By similar treatment as in Synthesis Example 1 except that one part of the compound (532) was changed to 1.7 parts of the following compound (538), 1.23 g of a compound (108) was obtained as brown crystal.

λmax (EtOH: 417 nm)

¹H-NMR (PPM: d6-DMSO): 7.04(d.arom.2H), 7.17-7.41(m.arom.7H), 7.48(m.arom.4H), 7.66-7.78(m.arom.7H), 7.98(d.arom.2H), 8.17(s.—CH═.1H)

Example 9

A dye was dissolved in EtOH in concentration of 3.2×10⁻⁴M. In this solution was dipped a porous substrate (a semiconductor thin film electrode obtained by sintering porous titanium oxide on transparent, electric conductive glass electrode at 450° C. for 30 minutes) at room temperature for from 3 hours to over night to carry a dye, followed by washing with a solvent and drying to obtain a photoelectric conversion device of a semiconductor thin film sensitized with a dye. In Examples 19 and 20, each concentration of two kinds of dyes in an EtOH solution was adjusted to be 1.6×10⁻⁴ M to similarly obtain a photoelectric conversion device by carrying two kinds of dyes. In Examples 16, 19 and 20, an aqueous solution of 0.2 M of titanium tetrachloride was added dropwise onto thin film part of titanium oxide of a thin film semiconductor electrode, followed by standing still at room temperature for 24 hours, washing with water and firing again at 450° C. for 30 minutes to similarly carry a dye using a thin film semiconductor electrode treated with titanium tetrachloride. Further in Example 15, on carrying a dye on a semiconductor thin film, cholic acid was added as an inclusion compound in 3×10⁻² M to prepare the above dye solution to obtain a cholic acid-treated dye-sensitized semiconductor thin film. Electric conductive glass sputtered with platinum at the surface was fixed so as to sandwich this, and into clearance thereof, a solution containing an electrolyte was poured. The electrolyte solution was used by dissolving iodine/lithiumiodine/1,2-dimethyl-3-n-propylimidazol iumodide/t-butylpyridine into 3-methoxypropionitrile in 0.1M/0.1M/0.6M/1M, respectively.

Effective area of a cell to be measured was 0.25 cm². As a light source, a 500 W xenon lamp was used so that 100 mW/cm² could be obtained through AM (air mass) 1.5 filter. Short-circuit current, release voltage and conversion efficiency were measured using a potentio-galvanostat.

TABLE 12 Short-circuit Release Conversion Treatment of Organic current votage efficiency thin film with Presence of Example dye (mA/cm²) (V) (%) TiCl₄ cholic acid 9 14 9.2 0.67 4.3 non-treated absent 10 91 10.0 0.65 4.6 non-treated absent 11 108 8.7 0.69 4.3 non-treated absent 12 197 8.6 0.66 4.0 non-treated absent 13 205 9.4 0.68 4.5 non-treated absent 14 246 9.8 0.67 4.6 non-treated absent 15 246 11.8 0.67 5.6 non-treated present 16 246 13.5 0.67 6.5 treated absent 17 272 8.6 0.64 3.8 non-treated absent 18 523 8.9 0.67 4.2 non-treated absent 19  14 + 108 10.1 0.67 4.9 treated absent 20 246 + 523 13.9 0.66 6.6 treated absent

As is clear from Table 12, by using a photoelectric conversion device sensitized with a methine dye represented by Formula (1), visible ray can effectively be converted to electricity.

Industrial Applicability

In a dye-sensitized photoelectric conversion device of the present invention, by using a dye with specified partial structure, a solar cell with high conversion efficiency and high stability could be provided. Furthermore, by using fine oxide semiconductor particles sensitized with two or more kinds of dyes used in combination, enhancement of conversion efficiency could be observed. 

1. A photoelectric conversion device, comprising fine oxide semiconductor particles sensitized with a methine dye represented by Formula (1):

(in Formula (1), each of R₁ and R₂ represents a hydrogen atom, an optionally substituted aromatic residual group, an optionally substituted aliphatic hydrocarbon residual group or an acyl group, provided that R₁ and R₂ may form an optionally substituted ring, by bonding with each other or with a benzene ring a₁; m₁ is an integer of 0 to 7; n₁ is an integer of 1 to 7; X₁ represents a carboxyl group; each of A₁ and A₂ represents independently an optionally substituted aromatic residual group, a hydroxyl group, a phosphate group, a cyano group, a hydrogen atom, a halogen atom, an optionally substituted aliphatic hydrocarbon residual group, a carboxyl group, a carboamido group, an alkoxycarbonyl group or an acyl group, provided that when n₁ is not smaller than 2 and A₁ and A₂ are present in plural, each of A₁ and each of A₂ may be the same or different from each other; an optionally substituted ring optionally formed using multiple substituents selected from A₁ or each of A₁ when A₁ is present in plural, and A₂ or each of A₂ when A₂ is present in plural, along with X₁; Y₁ represents a sulfur atom, a selenium atom, a tellurium atom and CR₃R₄ or NR₅, wherein R₃ and R₄ represent a hydrogen atom, a halogen atom, an amide group, a hydroxyl group, a cyano group, a nitro group, an alkoxyl group, an acyl group, a substituted or unsubstituted amino group, an optionally substituted aliphatic hydrocarbon residual group or an optionally substituted aromatic residual group; R₅ represents a hydrogen atom, an optionally substituted aromatic residual group, an optionally substituted aliphatic hydrocarbon residual group or an acyl group; when m₁ is not smaller than 2 and Y₁ is present in plural, each of Y₁ optionally is the same or different from each other; a benzene ring a₁ optionally has one or plural substituents, including a halogen atom, an amide group, a hydroxyl group, a cyano group, a nitro group, an alkoxyl group, an acyl group, a substituted or unsubstituted amino group, an optionally substituted aliphatic hydrocarbon residual group or an optionally substituted aromatic residual group; a benzene ring a₁ optionally also forms an optionally substituted ring by bonding of plural substituents themselves; and a ring b₁ optionally has one or plural substituents including a halogen atom, an alkoxyl group, an acyl group, an optionally substituted aliphatic hydrocarbon residual group or an optionally substituted aromatic residual group; and a ring b₁ optionally forms an optionally substituted ring by bonding of plural substituents themselves); provided that when m1 is 0, R1 represents the following formula (3′) and R2 represents the following formula (3″):

wherein a benzene ring c₂ optionally has one or plural substituents including a halogen atom, an amide group, a hydroxyl group, an alkoxyl group, a substituted or unsubstituted amino group, an optionally substituted aliphatic hydrocarbon residual group or an optionally substituted aromatic residual group; and a benzene ring c₂ optionally forms an optionally substituted ring by bonding of said plural substituents themselves; and R₁₁ and R₁₂ are each independently a substituted or unsubstituted aromatic residual group).
 2. The photoelectric conversion device according to claim 1, wherein a methine dye represented by Formula (1) is a compound with R₁ and R₂ being an optionally substituted aromatic residual group in Formula (1).
 3. The photoelectric conversion device according to claim 1, comprising an oxide semiconductor sensitized with one kind or more of a methine dye represented by Formula (1) and with a metal complex and/or an organic dye having a structure other than Formula (1).
 4. The photoelectric conversion device according to claim 1, wherein fine oxide semiconductor particles contain titanium dioxide as an essential component.
 5. The photoelectric conversion device according to claim 1, wherein fine oxide semiconductor particles contain zinc or tin as an essential component as a metal component.
 6. The photoelectric conversion device according to claim 1, wherein onto fine oxide semiconductor particles a dye is carried in the presence of an inclusion compound.
 7. A solar cell comprising a photoelectric conversion device according to claim
 1. 